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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease cone rod dystrophy
Comorbidity C0034951|refractive error
Sentences 2
PubMedID- 25883087 Objective: to determine the refractive error in patients with autosomal recessive retinitis pigmentosa (arrp) caused by rp1 mutations and to compare it with that of other genetic subtypes of rp.
PubMedID- 24146540 The incidence of myopic refractive errors in patients with retinitis pigmentosa (rp) is 75%, while patients with the x-linked form of rp reach 95% [18].

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